Awareness screening and referral patterns among pediatricians in the United States related to early clinical features of spinal muscular atrophy (SMA)

BACKGROUND: Spinal Muscular Atrophy (SMA), a leading genetic cause of death in infants, is an autosomal recessive neuromuscular disease characterized by progressive muscle weakness and atrophy. While early diagnosis of SMA is critical to modifying disease progression and improving outcomes, serious...

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Detalles Bibliográficos
Autores principales: Curry, Mary, Cruz, Rosángel, Belter, Lisa, Schroth, Mary, Lenz, Megan, Jarecki, Jill
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8127310/
https://www.ncbi.nlm.nih.gov/pubmed/34001052
http://dx.doi.org/10.1186/s12887-021-02692-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8127310/
https://www.ncbi.nlm.nih.gov/pubmed/34001052
http://dx.doi.org/10.1186/s12887-021-02692-2

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